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FDA 510(k)

FH 101, FH 202 & FH 303 FIBER HEMOFILTER

K-Number: K830284 · 1983-03-02

ApplicantGambro, Inc.
Decision Date1983-03-02
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FH 101, FH 202 & FH 303 FIBER HEMOFILTER is the device name listed in this FDA 510(k) record. The listed applicant is Gambro, Inc.. It received FDA 510(k) clearance on 1983-03-02 under 510(k) number K830284. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FH 101, FH 202 & FH 303 FIBER HEMOFILTER?

FH 101, FH 202 & FH 303 FIBER HEMOFILTER is a medical device that received FDA 510(k) clearance on 1983-03-02. The listed applicant is Gambro, Inc.. The 510(k) number is K830284.

When did FH 101, FH 202 & FH 303 FIBER HEMOFILTER receive FDA 510(k) clearance?

FH 101, FH 202 & FH 303 FIBER HEMOFILTER received FDA 510(k) clearance on 1983-03-02, under 510(k) number K830284.

Who is the listed applicant for FH 101, FH 202 & FH 303 FIBER HEMOFILTER?

The FDA 510(k) record lists Gambro, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FH 101, FH 202 & FH 303 FIBER HEMOFILTER?

The FDA product code for FH 101, FH 202 & FH 303 FIBER HEMOFILTER is KDI.

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Other records listing Gambro, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K083158EXALIS, SOFTWARE VERSION 1.15K070643PHOENIX HEMODIALYSIS DELIVERY SYSTEM, VERSION 3.35K032431PRISMA M60/M100 SETSK896758GAMBRO BICARBONATE MONITOR BCM 10-3K896757GAMBRO AK-10 DIALYSIS SYSTEM FOR HIGH FLOWSK902481GAMBRO ALWALL GFS PLUS 11, 16 & 20 HOLLOW FIBER

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Related Devices (Code: KDI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261267Careflux H60;Careflux H70;Careflux V500Fresenius Medical Care Renal Therapies Group, LLCK252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLCK260533ELISIO™-HNipro Medical CorporationK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLCK253412Tablo Hemodialysis System (PN-0008000, PN-0006000U)Outset Medical, Inc.K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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